Plasticity of Surface Structures and beta(2)-Adrenergic Receptor Localization in Failing Ventricular Cardiomyocytes During Recovery From Heart Failure

Background-Cardiomyocyte surface morphology and T-tubular structure are significantly disrupted in chronic heart failure, with important functional sequelae, including redistribution of sarcolemmal beta(2)-adrenergic receptors (beta(2)AR) and localized secondary messenger signaling. Plasticity of these changes in the reverse remodeled failing ventricle is unknown. We used AAV9.SERCA2a gene therapy to rescue failing rat hearts and measured z-groove index, T-tubule density, and compartmentalized beta(2)AR-mediated cAMP signals, using a combined nanoscale scanning ion conductance microscopy-Forster resonance energy transfer technique. Methods and Results-Cardiomyocyte surface morphology, quantified by z-groove index and T-tubule density, was normalized in reverse-remodeled hearts after SERCA2a gene therapy. Recovery of sarcolemmal microstructure correlated with functional beta(2)AR redistribution back into the z-groove and T-tubular network, whereas minimal cAMP responses were initiated after local beta(2)AR stimulation of crest membrane, as observed in failing cardiomyocytes. Improvement of beta(2)AR localization was associated with recovery of beta AR-stimulated contractile responses in rescued cardiomyocytes. Retubulation was associated with reduced spatial heterogeneity of electrically stimulated calcium transients and recovery of myocardial BIN-1 and TCAP protein expression but not junctophilin-2. Conclusions-In summary, abnormalities of sarcolemmal structure in heart failure show plasticity with reappearance of z-grooves and T-tubules in reverse-remodeled hearts. Recovery of surface topology is necessary for normalization of beta(2)AR location and signaling responses. (Circ Heart Fail. 2012;5:357-365.)